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The activation of these catalysts under H 2, produces cyclooctane, which is usually discarded or burnt: C 8 H 12 + 2 H 2 → C 8 H 16. Cyclooctane participates in no reactions except those typical of other saturated hydrocarbons, combustion and free radical halogenation. Work in 2009 on alkane functionalisation, using peroxides such as dicumyl ...
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
Norbornane (also called bicyclo[2.2.1]heptane). Unsubstituted cycloalkanes that contain a single ring in their molecular structure are typically named by adding the prefix "cyclo" to the name of the corresponding linear alkane with the same number of carbon atoms in its chain as the cycloalkane has in its ring.
1,5-Cyclooctadiene (also known as cycloocta-1,5-diene) is a cyclic hydrocarbon with the chemical formula C 8 H 12, specifically [−(CH 2) 2 −CH=CH−] 2.. There are three configurational isomers with this structure, that differ by the arrangement of the four C–C single bonds adjacent to the double bonds.
The CRC Handbook of Chemistry and Physics is a comprehensive one-volume reference resource for science research. First published in 1914, it is currently (as of 2024) in its 105th edition, published in 2024.
1,3,5,7-Cyclooctatetraene (COT) is an unsaturated derivative of cyclooctane, with the formula C 8 H 8.It is also known as [8]annulene.This polyunsaturated hydrocarbon is a colorless to light yellow flammable liquid at room temperature.
9-Borabicyclo[3.3.1]nonane or 9-BBN is an organoborane compound. This colourless solid is used in organic chemistry as a hydroboration reagent.The compound exists as a hydride-bridged dimer, which easily cleaves in the presence of reducible substrates.
Print/export Download as PDF; Printable version; In other projects ... Density: 0.871 g/cm 3: Melting point: 9 to 10 °C (48 to 50 °F; 282 to 283 K)